Work

A Novel Inherited Mutation of SCN8A in a Korean Family with Benign Familial Infantile Epilepsy Using Diagnostic Exome Sequencing.

Year: 2017

Type: article

Source: PubMed

Authors: Ji Yoon Han, Ja Hyun Jang, In Goo Lee, Soyoung Shin, Joonhong Park

Institution: Catholic University of Korea

Language: English

Topic: Epilepsy research and treatment

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2785159869

FWCI: 1.704

Cites:

Cited by: 16

Related to: 10